Weight | 172.209 g/mol |
---|---|
Formula | C6H8N2O2S |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2-Aminobenzenesulfonamide (3306-62-5)
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- Oxidative synthesis of quinazolinones and benzothiadiazine 1,1-dioxides from 2-aminobenzamide and 2-aminobenzenesulfonamide with benzyl alcohols and aldehydes (RSC Advances, 2014)
- Facile Syntheses of 2H-1,2,4-Benzothiadiazine 1,1-Dioxides and 4-Oxo-3,4-dihydroquinazolines from 2-Aminobenzenesulfonamide or 2-Aminobenzamide and Aldehydes in the Presence of Sodium Hydrogen Sulfite (Synthesis, 1981)
- A comparison of ring-chain tautomerism in heterocycles derived from 2-aminobenzenesulfonamide and anthranilamide (Tetrahedron, 2005)
- A Convenient Synthesis of 2H-1,2,4-Benzothiadiazine 1,1-Dioxides from 2-Aminobenzenesulfonamide and Carboxylic Acids by using Polyphosphoric Acid Trimethylsilyl Ester as Condensing Agent (Synthesis, 1983)
- Recyclization of 2-imino-2H-1-benzopyrans under the influence of nucleophilic reagents. 2. Reaction of 2-iminocoumarin-3-carboxamides witho-aminobenzenesulfonamide (Chemistry of Heterocyclic Compounds, 1998)
- Development of certain new 2-substituted-quinazolin-4-yl-aminobenzenesulfonamide as potential antitumor agents (European Journal of Medicinal Chemistry, 2016)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)N)S(=O)(=O)N
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InChIKeyYAZSBRQTAHVVGE-UHFFFAOYSA-N
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